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PLEKHG5 antibody (Pleckstrin Homology Domain Containing, Family G (With RhoGef Domain) Member 5) (N-Term)

Details for Product anti-PLEKHG5 Antibody No. ABIN347101, Supplier: Log in to see
Antigen
  • PLEKHG5
  • plekhg5
  • si:ch211-15p9.7
  • syx
  • syx-a
  • DSMA4
  • GEF720
  • Syx
  • Tech
  • BC023181
  • mKIAA0720
  • pleckstrin homology domain containing, family G (with RhoGef domain) member 5
  • pleckstrin homology domain containing, family G (with RhoGef domain) member 5a
  • PLEKHG5
  • plekhg5a
  • plekhg5
  • Plekhg5
Alternatives
anti-Human PLEKHG5 antibody for Immunohistochemistry
Epitope
N-Term
13
10
9
8
2
2
1
Reactivity
Human
39
4
4
Host
Rabbit
27
12
Clonality
Polyclonal
Conjugate
This PLEKHG5 antibody is un-conjugated
3
3
3
3
3
3
Application
Immunohistochemistry (IHC), ELISA, Western Blotting (WB)
37
29
10
5
3
1
1
Options
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Immunogen Synthetic peptide derived from N terminal region of PLEKHG5
Isotype IgG
Specificity Reacts with 98-105 kDa of human PLEKHG5
Purification Antiserum
Alternative Name PLEKHG5 (PLEKHG5 Antibody Abstract)
Background PLEKHG5 is involved in the control of neuronal cell differentiation. It activates NF-kappa B and RHOA.
Gene ID 57449
UniProt O94827
Research Area Chromatin and Nuclear Signaling
Pathways Neurotrophin Signaling Pathway
Application Notes

Working dilution: Optimal dilution should be determined by the end user.
The following are guidelines only :
- IHC : 1/50 to 1/200 - WB : 1/200 to 1/1 000

Restrictions For Research Use only
Format Lyophilized
Reconstitution Must be reconstituted in distilled water.
Storage 4 °C/-20 °C
Storage Comment Lyophilized powder stable for a minimum of 2 years at -20°C. Store reconstituted antibodies at +4°C. For extended periods store in aliquots at -20°C. Antibodies are guaranteed for 6 month from date of receipt.
Expiry Date 24 months
Background publications Maystadt, Rezsöhazy, Barkats, Duque, Vannuffel, Remacle, Lambert, Najimi, Sokal, Munnich, Viollet, Verellen-Dumoulin: "The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset." in: American journal of human genetics, Vol. 81, Issue 1, pp. 67-76, 2007 (PubMed).

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